A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573792



Internal ID16361201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89852186..89852649hg38UCSC Ensembl
Innerchr16:89918594..89919057hg19UCSC Ensembl
Innerchr16:88446095..88446558hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38464
hg19464
hg18464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5331n54
Supporting Variantsnssv863587, nssv863588, nssv863586, nssv863591, nssv863589, nssv863585, nssv863590
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573792
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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